MELAS: An original case and clinical criteria for diagnosis
- 1 January 1992
- journal article
- case report
- Published by Elsevier in Neuromuscular Disorders
- Vol. 2 (2) , 125-135
- https://doi.org/10.1016/0960-8966(92)90045-8
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- MELAS: Clinical features, biochemistry, and molecular geneticsAnnals of Neurology, 1992
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)Neurology, 1992
- A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1991
- Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)The Lancet, 1991
- Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesThe Lancet, 1991
- A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)Biochemical and Biophysical Research Communications, 1990
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaNeurology, 1975